Canonical Allele Identifier: CA1937420480

Gene: HABP2

Linked Data

• dbSNP Id: rs1845298037

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571047C>T , CM000672.2:g.113571047C>T	GRCh38
NC_000010.10:g.115330806C>T , CM000672.1:g.115330806C>T	GRCh37
NC_000010.9:g.115320796C>T	NCBI36
NG_008956.1:g.23029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3242C>T MANE Select	ENSP00000277903.4:n.107-3242C>T
ENST00000351270.3:c.107-3242C>T	ENSP00000277903.4:n.107-3242C>T
ENST00000542051.5:c.29-3242C>T	ENSP00000443283.1:n.29-3242C>T
NM_001177660.1:c.29-3242C>T	NP_001171131.1:n.29-3242C>T
NM_004132.3:c.107-3242C>T	NP_004123.1:n.107-3242C>T
NM_001177660.2:c.29-3242C>T	NP_001171131.1:n.29-3242C>T
NM_004132.4:c.107-3242C>T	NP_004123.1:n.107-3242C>T
NM_004132.5:c.107-3242C>T MANE Select	NP_004123.1:n.107-3242C>T
NM_001177660.3:c.29-3242C>T	NP_001171131.1:n.29-3242C>T